NDC 68084-343 – Topiramate
Topiramate 50 mg/1 · Tablet, Film Coated · Oral
Product NDC68084-343
Product details
- Brand name
- Topiramate
- Generic name
- Topiramate
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078235
- Marketed since
- November 8, 2019
- Listing expires
- December 31, 2026
Active ingredients
- Topiramate 50 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68084-343-01 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-343-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-343-11) | Nov 8, 2019 |
Recalls mentioning this NDC
- D-1645-2012 Aug 22, 2012 · Class III
Labeling: Label Mix-Up: A typographical error in the product form on the carton label incorrectly lists the configuration as 30 "Capsules" (3 x 10) rather than "Tablets".
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